2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
95%
- Product Code: 51142
CAS:
135944-08-0
| Molecular Weight: | 413.47 g./mol | Molecular Formula: | C₂₆H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00273476 | |
| Melting Point: | 177-181°C | Boiling Point: | 658°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis, where it allows for the stepwise addition of amino acids to build peptides. The Fmoc group can be easily removed under mild basic conditions, making it a preferred choice for creating complex peptides and proteins. Its application is crucial in pharmaceutical research, biotechnology, and the development of therapeutic peptides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,591.00 |
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2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis, where it allows for the stepwise addition of amino acids to build peptides. The Fmoc group can be easily removed under mild basic conditions, making it a preferred choice for creating complex peptides and proteins. Its application is crucial in pharmaceutical research, biotechnology, and the development of therapeutic peptides.
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